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La variabilidad genética en la asociación esclerosis múltiple y el virus Epstein-Barr

Multiple sclerosis is a neurodegenerative and autoimmune disease of the central nervous system that mainly affects young people, especially women; its origin has been associated with infection caused by the Epstein-Barr virus. However, not all people who have suffered infection by this virus develop...

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Autor principal: Rivera-Silva, Gerardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Mexicano del Seguro Social 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10396045/
https://www.ncbi.nlm.nih.gov/pubmed/35816619
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author Rivera-Silva, Gerardo
author_facet Rivera-Silva, Gerardo
author_sort Rivera-Silva, Gerardo
collection PubMed
description Multiple sclerosis is a neurodegenerative and autoimmune disease of the central nervous system that mainly affects young people, especially women; its origin has been associated with infection caused by the Epstein-Barr virus. However, not all people who have suffered infection by this virus develop multiple sclerosis, so it would be important to know the role of genetic variability, especially the individual allelic variability of the human leukocyte antigen; as well as to determine the molecular mechanisms and the immunological links of the virus when it remains latent inside the B lymphocytes. Based on the above, it could be defined if the virus is a necessary condition to develop the disease or if there are other factors that need to be present, and thus be able to establish specific prevention and treatment strategies. But the most relevant thing is that the virus is a present condition to develop multiple sclerosis and is potentially preventable through the design of the respective vaccine.
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spelling pubmed-103960452023-08-04 La variabilidad genética en la asociación esclerosis múltiple y el virus Epstein-Barr Rivera-Silva, Gerardo Rev Med Inst Mex Seguro Soc Editorial Multiple sclerosis is a neurodegenerative and autoimmune disease of the central nervous system that mainly affects young people, especially women; its origin has been associated with infection caused by the Epstein-Barr virus. However, not all people who have suffered infection by this virus develop multiple sclerosis, so it would be important to know the role of genetic variability, especially the individual allelic variability of the human leukocyte antigen; as well as to determine the molecular mechanisms and the immunological links of the virus when it remains latent inside the B lymphocytes. Based on the above, it could be defined if the virus is a necessary condition to develop the disease or if there are other factors that need to be present, and thus be able to establish specific prevention and treatment strategies. But the most relevant thing is that the virus is a present condition to develop multiple sclerosis and is potentially preventable through the design of the respective vaccine. Instituto Mexicano del Seguro Social 2022 /pmc/articles/PMC10396045/ /pubmed/35816619 Text en © 2023 Revista Médica del Instituto Mexicano del Seguro Social. https://creativecommons.org/licenses/by-nc-nd/4.0/Esta obra está bajo una Licencia Creative Commons Atribución-NoComercial-SinDerivar 4.0 Internacional.
spellingShingle Editorial
Rivera-Silva, Gerardo
La variabilidad genética en la asociación esclerosis múltiple y el virus Epstein-Barr
title La variabilidad genética en la asociación esclerosis múltiple y el virus Epstein-Barr
title_full La variabilidad genética en la asociación esclerosis múltiple y el virus Epstein-Barr
title_fullStr La variabilidad genética en la asociación esclerosis múltiple y el virus Epstein-Barr
title_full_unstemmed La variabilidad genética en la asociación esclerosis múltiple y el virus Epstein-Barr
title_short La variabilidad genética en la asociación esclerosis múltiple y el virus Epstein-Barr
title_sort la variabilidad genética en la asociación esclerosis múltiple y el virus epstein-barr
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10396045/
https://www.ncbi.nlm.nih.gov/pubmed/35816619
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